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Improved emission of Yb() ions in triazacyclononane-based macrocyclic ligands compared to cyclen-based ones
Yb( iii ) complexes based on ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core were synthesised. The complexes carry a 4-methoxymethyl-substituted carbostyril chromophore that serves as a light-harvesting antenna. The ligands supply 5 nitrogen and 3 oxygen donors via 1 methylenecarboxam...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2022-11, Vol.51 (43), p.16596-1664 |
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container_start_page | 16596 |
container_title | Dalton transactions : an international journal of inorganic chemistry |
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creator | Kiraev, Salauat R Mathieu, Emilie Kovacs, Daniel Wells, Jordann A. L Tomar, Monika Andres, Julien Borbas, K. Eszter |
description | Yb(
iii
) complexes based on ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core were synthesised. The complexes carry a 4-methoxymethyl-substituted carbostyril chromophore that serves as a light-harvesting antenna. The ligands supply 5 nitrogen and 3 oxygen donors
via
1 methylenecarboxamide and 2 picolinate donors, creating +1 charged complexes with an octadentate binding environment. The electronic properties of the picolinates are modulated by varying the substitution at the 4 position with OMe, H, Cl, or CF
3
. Cyclic voltammetry indicated that the tacn-based Yb(
iii
) complexes were easier to reduce than the analogous cyclen complexes. The first reductive event is likely picolinate-centred, followed by the formation of further reduced species. Antenna excitation yielded Yb(
iii
) luminescence in the near-infrared (NIR) region in all cases. The antenna photophysical properties were consistent with intraligand photoinduced electron transfer from the excited carbostyril to the picolinate groups. The relative quantum yields of Yb(
iii
) luminescence were determined. The lowest value was obtained for the complex with the most efficient antenna-to-picolinate photoinduced electron transfer. Despite intraligand electron transfer quenching of the antenna, the tacn-based Yb complexes were more emissive than their cyclen analogues, highlighting the influence of the ligand structure on the luminescence properties of NIR emissive lanthanide(
iii
) ions.
Yb(
iii
) complexes were synthesised from ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core. Tacn-based compounds equipped with 2 picolinate arms were more emissive than their tricarboxamide-cyclen analogues carrying the same antenna. |
doi_str_mv | 10.1039/d2dt02266d |
format | article |
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iii
) complexes based on ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core were synthesised. The complexes carry a 4-methoxymethyl-substituted carbostyril chromophore that serves as a light-harvesting antenna. The ligands supply 5 nitrogen and 3 oxygen donors
via
1 methylenecarboxamide and 2 picolinate donors, creating +1 charged complexes with an octadentate binding environment. The electronic properties of the picolinates are modulated by varying the substitution at the 4 position with OMe, H, Cl, or CF
3
. Cyclic voltammetry indicated that the tacn-based Yb(
iii
) complexes were easier to reduce than the analogous cyclen complexes. The first reductive event is likely picolinate-centred, followed by the formation of further reduced species. Antenna excitation yielded Yb(
iii
) luminescence in the near-infrared (NIR) region in all cases. The antenna photophysical properties were consistent with intraligand photoinduced electron transfer from the excited carbostyril to the picolinate groups. The relative quantum yields of Yb(
iii
) luminescence were determined. The lowest value was obtained for the complex with the most efficient antenna-to-picolinate photoinduced electron transfer. Despite intraligand electron transfer quenching of the antenna, the tacn-based Yb complexes were more emissive than their cyclen analogues, highlighting the influence of the ligand structure on the luminescence properties of NIR emissive lanthanide(
iii
) ions.
Yb(
iii
) complexes were synthesised from ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core. Tacn-based compounds equipped with 2 picolinate arms were more emissive than their tricarboxamide-cyclen analogues carrying the same antenna.</description><identifier>ISSN: 1477-9226</identifier><identifier>ISSN: 1477-9234</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d2dt02266d</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Chemical Sciences ; Chromophores ; Coordination chemistry ; Donors (electronic) ; Electron transfer ; Ligands ; Luminescence ; Near infrared radiation ; Optical properties</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2022-11, Vol.51 (43), p.16596-1664</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><rights>Attribution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-8ba4603b6151b4420141c6b0e1a364e4b13033f38e6ee1bd90f1befb24f1e64e3</citedby><cites>FETCH-LOGICAL-c421t-8ba4603b6151b4420141c6b0e1a364e4b13033f38e6ee1bd90f1befb24f1e64e3</cites><orcidid>0000-0002-9313-8679 ; 0000-0003-4020-7383 ; 0000-0002-0754-2668 ; 0000-0001-8111-5368 ; 0000-0003-2449-102X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04297267$$DView record in HAL$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-489081$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Kiraev, Salauat R</creatorcontrib><creatorcontrib>Mathieu, Emilie</creatorcontrib><creatorcontrib>Kovacs, Daniel</creatorcontrib><creatorcontrib>Wells, Jordann A. L</creatorcontrib><creatorcontrib>Tomar, Monika</creatorcontrib><creatorcontrib>Andres, Julien</creatorcontrib><creatorcontrib>Borbas, K. Eszter</creatorcontrib><title>Improved emission of Yb() ions in triazacyclononane-based macrocyclic ligands compared to cyclen-based ones</title><title>Dalton transactions : an international journal of inorganic chemistry</title><description>Yb(
iii
) complexes based on ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core were synthesised. The complexes carry a 4-methoxymethyl-substituted carbostyril chromophore that serves as a light-harvesting antenna. The ligands supply 5 nitrogen and 3 oxygen donors
via
1 methylenecarboxamide and 2 picolinate donors, creating +1 charged complexes with an octadentate binding environment. The electronic properties of the picolinates are modulated by varying the substitution at the 4 position with OMe, H, Cl, or CF
3
. Cyclic voltammetry indicated that the tacn-based Yb(
iii
) complexes were easier to reduce than the analogous cyclen complexes. The first reductive event is likely picolinate-centred, followed by the formation of further reduced species. Antenna excitation yielded Yb(
iii
) luminescence in the near-infrared (NIR) region in all cases. The antenna photophysical properties were consistent with intraligand photoinduced electron transfer from the excited carbostyril to the picolinate groups. The relative quantum yields of Yb(
iii
) luminescence were determined. The lowest value was obtained for the complex with the most efficient antenna-to-picolinate photoinduced electron transfer. Despite intraligand electron transfer quenching of the antenna, the tacn-based Yb complexes were more emissive than their cyclen analogues, highlighting the influence of the ligand structure on the luminescence properties of NIR emissive lanthanide(
iii
) ions.
Yb(
iii
) complexes were synthesised from ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core. Tacn-based compounds equipped with 2 picolinate arms were more emissive than their tricarboxamide-cyclen analogues carrying the same antenna.</description><subject>Chemical Sciences</subject><subject>Chromophores</subject><subject>Coordination chemistry</subject><subject>Donors (electronic)</subject><subject>Electron transfer</subject><subject>Ligands</subject><subject>Luminescence</subject><subject>Near infrared radiation</subject><subject>Optical properties</subject><issn>1477-9226</issn><issn>1477-9234</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0c9P2zAUB_BoAmkFdtkdyRIXOi2bf-Ekx4qygVSJC0PaybKdF3BJ7M5OiuCvxyGoaJz85PexZX9fln0l-AfBrPpZ07rHlApRf8pmhBdFXlHG93Y1FZ-zgxjXOCF8RmfZw1W3CX4LNYLOxmi9Q75Bf_XpHKU6IutQH6x6VubJtN55pxzkWsV0oFMm-HHbGtTaO-XqiIzvNiqkZu_R2AL3hr2DeJTtN6qN8OVtPcz-_Lq4Ob_MV9e_r84Xq9xwSvq81IoLzLQgZ0RzTjHhxAiNgSgmOHBNGGasYSUIAKLrCjdEQ6MpbwgkwA6z79O98RE2g5abYDsVnqRXVi7t7UL6cCeHQfKywiVJfD7xe9X-Zy8XKznuYU6rgopiO9rTyabQ_g0Qe5lSM9C2KRY_REmTSykXlCV68oGu_RBc-nhSjFaCVOWovk0qZRljgGb3AoLlOFK5pMub15EuEz6ecIhm595Hzl4ANx6c0A</recordid><startdate>20221108</startdate><enddate>20221108</enddate><creator>Kiraev, Salauat R</creator><creator>Mathieu, Emilie</creator><creator>Kovacs, Daniel</creator><creator>Wells, Jordann A. L</creator><creator>Tomar, Monika</creator><creator>Andres, Julien</creator><creator>Borbas, K. Eszter</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-9313-8679</orcidid><orcidid>https://orcid.org/0000-0003-4020-7383</orcidid><orcidid>https://orcid.org/0000-0002-0754-2668</orcidid><orcidid>https://orcid.org/0000-0001-8111-5368</orcidid><orcidid>https://orcid.org/0000-0003-2449-102X</orcidid></search><sort><creationdate>20221108</creationdate><title>Improved emission of Yb() ions in triazacyclononane-based macrocyclic ligands compared to cyclen-based ones</title><author>Kiraev, Salauat R ; Mathieu, Emilie ; Kovacs, Daniel ; Wells, Jordann A. L ; Tomar, Monika ; Andres, Julien ; Borbas, K. Eszter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-8ba4603b6151b4420141c6b0e1a364e4b13033f38e6ee1bd90f1befb24f1e64e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chemical Sciences</topic><topic>Chromophores</topic><topic>Coordination chemistry</topic><topic>Donors (electronic)</topic><topic>Electron transfer</topic><topic>Ligands</topic><topic>Luminescence</topic><topic>Near infrared radiation</topic><topic>Optical properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kiraev, Salauat R</creatorcontrib><creatorcontrib>Mathieu, Emilie</creatorcontrib><creatorcontrib>Kovacs, Daniel</creatorcontrib><creatorcontrib>Wells, Jordann A. L</creatorcontrib><creatorcontrib>Tomar, Monika</creatorcontrib><creatorcontrib>Andres, Julien</creatorcontrib><creatorcontrib>Borbas, K. Eszter</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kiraev, Salauat R</au><au>Mathieu, Emilie</au><au>Kovacs, Daniel</au><au>Wells, Jordann A. L</au><au>Tomar, Monika</au><au>Andres, Julien</au><au>Borbas, K. Eszter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved emission of Yb() ions in triazacyclononane-based macrocyclic ligands compared to cyclen-based ones</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><date>2022-11-08</date><risdate>2022</risdate><volume>51</volume><issue>43</issue><spage>16596</spage><epage>1664</epage><pages>16596-1664</pages><issn>1477-9226</issn><issn>1477-9234</issn><eissn>1477-9234</eissn><abstract>Yb(
iii
) complexes based on ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core were synthesised. The complexes carry a 4-methoxymethyl-substituted carbostyril chromophore that serves as a light-harvesting antenna. The ligands supply 5 nitrogen and 3 oxygen donors
via
1 methylenecarboxamide and 2 picolinate donors, creating +1 charged complexes with an octadentate binding environment. The electronic properties of the picolinates are modulated by varying the substitution at the 4 position with OMe, H, Cl, or CF
3
. Cyclic voltammetry indicated that the tacn-based Yb(
iii
) complexes were easier to reduce than the analogous cyclen complexes. The first reductive event is likely picolinate-centred, followed by the formation of further reduced species. Antenna excitation yielded Yb(
iii
) luminescence in the near-infrared (NIR) region in all cases. The antenna photophysical properties were consistent with intraligand photoinduced electron transfer from the excited carbostyril to the picolinate groups. The relative quantum yields of Yb(
iii
) luminescence were determined. The lowest value was obtained for the complex with the most efficient antenna-to-picolinate photoinduced electron transfer. Despite intraligand electron transfer quenching of the antenna, the tacn-based Yb complexes were more emissive than their cyclen analogues, highlighting the influence of the ligand structure on the luminescence properties of NIR emissive lanthanide(
iii
) ions.
Yb(
iii
) complexes were synthesised from ligands with a 1,4,7-triazacyclononane (tacn) macrocyclic core. Tacn-based compounds equipped with 2 picolinate arms were more emissive than their tricarboxamide-cyclen analogues carrying the same antenna.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2dt02266d</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9313-8679</orcidid><orcidid>https://orcid.org/0000-0003-4020-7383</orcidid><orcidid>https://orcid.org/0000-0002-0754-2668</orcidid><orcidid>https://orcid.org/0000-0001-8111-5368</orcidid><orcidid>https://orcid.org/0000-0003-2449-102X</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Chemical Sciences Chromophores Coordination chemistry Donors (electronic) Electron transfer Ligands Luminescence Near infrared radiation Optical properties |
title | Improved emission of Yb() ions in triazacyclononane-based macrocyclic ligands compared to cyclen-based ones |
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